Reacción #1419

ord-c5d05c1fc29046a898bb31a5a6831fa6

Ecuación de reacción

O=N[O-].[Na+]
sodium nitrite
Cc1ccccc1
toluene
N[C@@H](Cc1ccccc1)C(=O)O
L-phenylalanine
[Br-].[K+]
potassium bromide
O=C(O)[C@@H](Br)Cc1ccccc1
(S)-α-Bromobenzenepropanoic acid

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónafter which the reaction mixture was extracted with ether (3×250 ml.)
  2. 2
    LavadoThe combined organic extracts were washed with water (100 ml.) and brine (50 ml.)
  3. 3
    Secadodried (anhydrous magnesium sulfate)
  4. 4
    Filtraciónfiltered
  5. 5
    Otroevaporated to dryness
  6. 6
    Otrodried in vacuo
  7. 7
    Otroto give 34.46 g

Procedimiento

A solution of L-phenylalanine (30.0 g., 0.175 mole) and potassium bromide (73.5 g., 0.618 mole) in 2.5N sulfuric acid (365 ml.) was cooled down to 0° (ice-salt bath) and treated portionwise with sodium nitrite (19.3 g., 0.28 mole) over a period of 1.0 hour. Stirring was continued for 1.0 hour at 0° and at room temperature for 1.0 hour after which the reaction mixture was extracted with ether (3×250 ml.). The combined organic extracts were washed with water (100 ml.) and brine (50 ml.), dried (anhydrous magnesium sulfate), filtered, evaporated to dryness and dried in vacuo to give 34.46 g., of product; Rf =0.45 (toluene:acetic acid, 95:5).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723602uspto-grants-1998_03